E.P. Weijers
Energy Research Centre of the Netherlands
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Featured researches published by E.P. Weijers.
Environmental Health Perspectives | 2011
Hanna Boogaard; Nicole A.H. Janssen; Paul Fischer; Gerard Kos; E.P. Weijers; Flemming R. Cassee; Saskia C. van der Zee; Jeroen J. de Hartog; Bert Brunekreef; Gerard Hoek
Background: Measuring the oxidative potential of airborne particulate matter (PM) may provide a more health-based exposure measure by integrating various biologically relevant properties of PM into a single predictor of biological activity. Objectives: We aimed to assess the contrast in oxidative potential of PM collected at major urban streets and background locations, the associaton of oxidative potential with other PM characteristics, and the oxidative potential in different PM size fractions. Methods: Measurements of PM with aerodynamic diameter ≤ 10 μm (PM10), PM with aerodynamic diameter ≤ 2.5 μm (PM2.5), soot, elemental composition, and oxidative potential of PM were conducted simultaneously in samples from 8 major streets and 10 urban and suburban background locations in the Netherlands. Six 1-week measurements were performed at each location over a 6-month period in 2008. Oxidative potential was measured as the ability to generate hydroxyl radicals in the presence of hydrogen peroxide in all PM10 samples and a subset of PM2.5 samples. Results: The PM10 oxidative potential of samples from major streets was 3.6 times higher than at urban background locations, exceeding the contrast for PM mass, soot, and all measured chemical PM characteristics. The contrast between major streets and suburban background locations was even higher (factor of 6.5). Oxidative potential was highly correlated with soot, barium, chromium, copper, iron, and manganese. Oxidative potential of PM10 was 4.6 times higher than the oxidative potential of PM2.5 when expressed per volume unit and 3.1 times higher when expressed per mass unit. Conclusions: The oxidative potential of PM near major urban roads was highly elevated compared with urban and suburban background locations, and the contrast was greater than that for any other measured PM characteristic.
Atmospheric Chemistry and Physics | 2010
E.P. Weijers; M. Schaap; L. Nguyen; J. Matthijsen; H. A. C. Denier van der Gon; H.M. ten Brink; R. Hoogerbrugge
To develop mitigation strategies for reducing concentrations of both PM2.5 and PM10, the origin of particulate matter (PM) needs to be established. An intensive, one-year measurement campaign from August 2007 to August 2008 was carried out to determine the composition of PM 10 and PM2.5 at five locations in the Netherlands, aiming at reducing the uncertainties on the origin of PM. Generally, a considerable conformity in the chemical composition of PM 2.5 (and PM10) is observed. From all constituents present in PM 2.5, the secondary inorganic aerosol is the most dominant (42– 48%), followed by the total carbonaceous matter (22–37%). Contributions from sea salt (maximum 8%), mineral dust and metals (maximum 5%) are relatively low. For the first time, a detailed overview of the composition of the coarse fraction can be presented. Compared to the fine fraction, contributions of sea salt, mineral dust and metals are larger resulting in a more balanced distribution between the various constituents. Through mass closure a considerable part of the PM mass could be defined (PM 2.5: 80–94%). The chemical distribution on days with high PM levels shows a distinct increase in nitrate as well as in the unaccounted mass. Contributions of the other constituents remain equal or are lower (sea salt) when expressed in percentages. A correspondence between nitrate and the unaccounted mass is observed hinting at the presence of water on the filters. The contribution from natural sources in the Netherlands (at a rural station) was estimated to be 19 to 24% for PM 10 and 13 to 17% for PM2.5. Correspondence to: E. P. Weijers ([email protected])
Epidemiology | 2013
Hanna Boogaard; Paul Fischer; Nicole A.H. Janssen; Gerard Kos; E.P. Weijers; Flemming R. Cassee; S.C. van der Zee; J. J. de Hartog; Kees Meliefste; Ming-Dong Wang; Bert Brunekreef; Gerard Hoek
Background: Air pollution has been associated with respiratory health effects. There is little direct evidence that reductions in air pollution related to abatement policies lead to actual improvement in respiratory health. We assessed whether a reduction in (traffic policy-related) air pollution concentrations was associated with changes in respiratory health. Methods: Air pollution concentrations and respiratory health were measured in 2008 and 2010 at eight busy urban streets and at four suburban background control locations. Respiratory function was assessed twice in 661 residents by spirometry and measurements of airway resistance. Nitric oxide (NO) in exhaled air was measured as a marker for airway inflammation. Results: Air pollution concentrations were lower in 2010 than in 2008. The declines in pollutants varied among locations, with the largest decline observed in a street with a large reduction in traffic intensity. In regression analyses adjusted for important covariates, reductions in concentrations of soot, NO2, NOx, Cu, and Fe were associated with increases in forced vital capacity (FVC) (∼1% increase per interquartile range [IQR] decline). Airway resistance decreased with a decline in particulate matter (PM10) and PM2.5 (9% per IQR), although these associations were somewhat less consistent. No associations were found with exhaled NO. Results were driven largely by one street where traffic-related air pollution showed the largest reduction. Forced expiratory volume and FVC improved by 3% to 6% in residents of this street compared with suburban background residents. This was accompanied by a suggestive reduction in airway resistance. Conclusions: Reductions in air pollution may lead to small improvements in respiratory function.
Atmospheric Environment | 2004
E.P. Weijers; Andrey Khlystov; Gerard Kos; Jan Willem Erisman
Atmospheric Environment | 2007
Mar Viana; Willy Maenhaut; H.M. ten Brink; Xuguang Chi; E.P. Weijers; X Querol; Andrés Alastuey; Pavel Mikuška; Zbyněk Večeřa
Atmospheric Environment | 2011
D. Mooibroek; M. Schaap; E.P. Weijers; R. Hoogerbrugge
Atmospheric Environment | 2011
Hanna Boogaard; Gerard Kos; E.P. Weijers; Nicole A.H. Janssen; Paul Fischer; Saskia C. van der Zee; Jeroen J. de Hartog; Gerard Hoek
Atmospheric Chemistry and Physics | 2010
M. Schaap; R. Otjes; E.P. Weijers
Science of The Total Environment | 2012
Hanna Boogaard; Nicole A.H. Janssen; Paul Fischer; Gerard Kos; E.P. Weijers; Flemming R. Cassee; Saskia C. van der Zee; Jeroen J. de Hartog; Kees Meliefste; Meng Wang; Bert Brunekreef; Gerard Hoek
Atmospheric Environment | 2016
Jelle Hofman; J. Staelens; Rebecca L. Cordell; C. Stroobants; Naděžda Zíková; Sarkawt M.L. Hama; Kevin P. Wyche; Gerard Kos; S. Van Der Zee; Kirsty Smallbone; E.P. Weijers; Paul S. Monks; Edward Roekens